The Effect of Peppermint Oil on Nausea, Vomiting and Retching in Cancer Patients Undergoing Chemotherapy
Chemotherapy Effect, Adverse Effect, Nursing Caries
About this trial
This is an interventional supportive care trial for Chemotherapy Effect focused on measuring Aromatherapy, Chemotherapy, Nausea-Vomiting, Nursing, Peppermint Oil
Eligibility Criteria
Inclusion Criteria: Patients who
- were aged ≥18 years,
- were able to understand Turkish language and to communicate in Turkish language,
- had cancer diagnosis,
- received chemotherapy treatment for -at least- the second time with similar chemotherapeutic agents,
- experienced nausea symptoms according to VAS
- were not pregnant and not intending pregnancy,
- had -at most- stage III cancer
- presented no psychiatric disorders,
- were not included in pre-implementation phase of the study were accepted to the study.
Exclusion Criteria:Patients who
- suffered from another disease that may affect nausea vomiting status,
- were allergic to or disturbed by smell of peppermint,
- were newly diagnosed, and receiving chemotherapy for the first time,
- received concomitant radiotherapy,
- received other complementary and integrative health practices during the treatment were not accepted to the study
Sites / Locations
- Nuriye EFE ERTURK
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
intervention group
control group
The patients in the intervention group applied peppermint oil (3%) on lips three times a day, during the five days following chemotherapy administration, in addition to the standard antiemetic treatments. The data were collected using a Patient Information Form, Rhodes Index of Nausea, Vomiting and Retching (INVR), Visual Analog Scale (VAS) Patient Nausea Severity Follow-up Form, Patient Watch Chart, and Oil Application Protocol. Besides, patients in the intervention group were questioned thoughts associated with peppermint oil application using individual in-depth interview method.
The control group underwent only the routine treatment.